Package 0832-5324-11

Brand: potassium chloride

Generic: potassium chloride
NDC Package

Package Facts

Identity

Package NDC 0832-5324-11
Digits Only 0832532411
Product NDC 0832-5324
Product ID 0832-5324_39990061-98d4-6669-e063-6394a90ae067
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0832-5324-11)

Marketing

Marketing Status
Marketed Since 2019-06-21
Brand potassium chloride
Generic potassium chloride
Sample Package No

Linked Drug Pages (1)

Potassium Chloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "39990061-98d4-6669-e063-6394a90ae067", "openfda": {"upc": ["0308325325113", "0308325324116"], "unii": ["660YQ98I10"], "rxcui": ["1801294", "1801298"], "spl_set_id": ["ad584ce4-a64d-4851-80e9-0eeedc0b9d06"], "manufacturer_name": ["Upsher-SmithLaboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (0832-5324-10)", "package_ndc": "0832-5324-10", "marketing_start_date": "20190621"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0832-5324-11)", "package_ndc": "0832-5324-11", "marketing_start_date": "20190621"}], "brand_name": "Potassium Chloride", "product_id": "0832-5324_39990061-98d4-6669-e063-6394a90ae067", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "0832-5324", "generic_name": "potassium chloride", "labeler_name": "Upsher-SmithLaboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Potassium Chloride", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA074726", "marketing_category": "ANDA", "marketing_start_date": "19981120", "listing_expiration_date": "20261231"}